No of openings : 05

Job Code: CRAOO1A

Experience: 1 to 4 yrs in Clinical Research Associative.

Job Description :

• Responsible for conduct of Qualification visit, Site Initiation Visit, Monitoring Visit and Closeouts visit.
• Would be the first point of contact for Communication with the Investigators and site personnel’s for the study assigned.
• Coordinate the movement of Laboratory samples if applicable.
• Ensuring the data entry/CRF filling, following-up visits of subjects as per the protocol.
• Prepares follow up letters and reports for the respective visits as per the SOPs and share with the site and Sponsor as required.
• Follow-up with the coordinator for the query resolution.
• To collect the collated Ethics Committee documents from CTA for EC submission as defined in site SOPs.
• To ensure that the interim safety reports, interim study reports are provided to EC as per the governed regulatory body.
• Preparation of power point presentations for investigator meetings and Site Initiation visits.
• Managing the CRC activities, and training them periodically.